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6-Hydroxy-1-methylquinolin-2(1H)-one, also known as 6-Hydroxy-1-methyl-1,2-dihydroquinolin-2-one, is a chemical compound with the molecular formula C10H9NO2. It is a derivative of quinolin-2(1H)-one and contains a hydroxyl group and a methyl group attached to the quinoline ring structure. 6-Hydroxy-1-methylquinolin-2(1H)-one has been studied for its potential pharmacological properties, including its anti-inflammatory and antioxidant activities. It has also been investigated for its potential use in the development of new drugs and therapies. Additionally, it has been used as a building block in the synthesis of various pharmaceutical and biologically active compounds. Overall, 6-Hydroxy-1-methylquinolin-2(1H)-one is a versatile compound with potential applications in the fields of pharmacology and medicinal chemistry.

69601-45-2

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69601-45-2 Usage

Uses

Used in Pharmaceutical Industry:
6-Hydroxy-1-methylquinolin-2(1H)-one is used as a building block for the synthesis of various pharmaceutical and biologically active compounds. Its unique structure and functional groups make it a valuable component in the development of new drugs and therapies.
Used in Medicinal Chemistry:
6-Hydroxy-1-methylquinolin-2(1H)-one is used as a research compound in medicinal chemistry for studying its potential pharmacological properties. Its anti-inflammatory and antioxidant activities have been of particular interest, as these properties could lead to the development of new treatments for various diseases and conditions.
Used in Drug Development:
6-Hydroxy-1-methylquinolin-2(1H)-one is used in the development of new drugs and therapies due to its potential pharmacological properties. Its ability to modulate various biological pathways and exhibit anti-inflammatory and antioxidant effects make it a promising candidate for further research and development in the pharmaceutical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 69601-45-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,6,0 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 69601-45:
(7*6)+(6*9)+(5*6)+(4*0)+(3*1)+(2*4)+(1*5)=142
142 % 10 = 2
So 69601-45-2 is a valid CAS Registry Number.

69601-45-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Hydroxy-1-methyl-2(1H)-quinolinone

1.2 Other means of identification

Product number -
Other names 5-METHOXYCARBONYL-2(1H)-PYRIDINONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:69601-45-2 SDS

69601-45-2Relevant academic research and scientific papers

Coumarin Derivatives Exert Anti-Lung Cancer Activity by Inhibition of Epithelial–Mesenchymal Transition and Migration in A549 Cells

Barreto, Emiliano,Bourguignon, Jean-Jacques,Dos Santos Carmo, Julianderson de Oliveira,Filho, José Maria Barbosa,Mendon?a-Junior, Francisco Jaime Bezerra,Rodarte, Renato Santos,Schmitt, Martine,Silva, Simone Lara de Omena,Souza, Tayhana Priscila Medeiros,da Silva, Camila Radelley Azevedo Costa,de Aquino, Thiago Mendon?a,de Araújo, Rodrigo Santos Aquino,de Mélo, Natália Barbosa,de Moura, Ricardo Olímpio

, (2022/01/24)

A series of coumarin derivatives and isosteres were synthesized from the reaction of triflic intermediates with phenylboronic acids, terminal alkynes, and organozinc compounds through palladium-catalyzed cross-coupling reactions. The in vitro cytotoxic ef

Heteroaryl quinolines as inhibitors of leukotriene biosynthesis

-

, (2008/06/13)

Compounds having the formula I: STR1 are inhibitors of leukotriene biosynthesis. These compounds are useful as anti-asthmatic, anti-allergic, anti-inflammatory, and cytoprotective agents. They are also useful in treating angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis, and allograft rejection and in preventing the formation of atherosclerotic plaques.

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